To provide a packaged medical device in which a medical device in a container is stably fixed and which can be easily opened. Specifically, provided is a packaged medical device comprising a container having an opening portion and a flange portion formed to extend outward in a peripheral portion of the opening portion, a medical device housed inside the container, and a lid member having a gas impermeable film and peelably heat-sealed to the flange portion, in which the inside of the container is set to a negative pressure to the atmospheric pressure so that the medical device is pressed by the lid member and the peel strength to the flange portion of the lid member is 2 to 50 N/in.

A temperature-protective package includes a rigid container configured to receive a temperature-sensitive product. A flexible liner is attached to the rigid container such that a pocket is formed between the rigid container and the flexible liner. Phase change material (PCM) is situated in the pocket. The PCM conforms to a contoured surface of the rigid container. In an alternative implementation, a temperature-sensitive package includes a pocket of PCM within a flexible liner. The flexible liner defines a preferred shape of the temperature-protective package. The flexible liner also defines an opening for receiving a product. The opening corresponds to the preferred shape. In one implementation, multiple flexible liners can be utilized to define the preferred shape and the opening.

A method of applying a buttress to a surgically cut and stapled site uses an end effector with a buttress applier cartridge assembly to load one or more buttress assemblies to the end effector. The buttress assemblies each include a buttress to support a staple formed therein as well an adhesive for adhering to the end effector. The adhesive of the buttress assemblies can include a pattern to assist in both attachment to the end effector and release from the end effector after cutting and stapling a tissue site. The buttress applier cartridge can include features that accommodate end effectors having various tip configurations, including straight tips and curved or bent tips.

An apparatus for inserting implants in a bone comprising a frame having a cartridge receiving chamber and a barrel. A cartridge defining a plurality of chambers is positioned in the cartridge receiving chamber so the chambers are selectively alignable with a longitudinal passage of the barrel. At least one instrument is positioned in one of the chambers, and a plurality of implants is positioned in the other chambers. A drive assembly is engageable with the instrument and the implants. The drive assembly is slidably and rotatably disposed in the frame and is moveable between a retracted position, an engaging position wherein the distal end of the drive assembly is positioned to engage the selected one of the instrument and the implants, and an extended position wherein the drive assembly extends through the chamber to transport the selected one of the instrument or the implant from the chamber to the distal end of the barrel.

In one aspect of the present disclosure, a tissue marking system is provided that includes a container and an applicator. The applicator is in the container and is removable therefrom. The applicator includes a tip, a reservoir containing sterile tissue marking dye, and a valve. The valve is configured to open and permit sterile tissue marking dye to flow from the reservoir to the tip of the applicator in response to the tip being pressed against a priming surface. In one embodiment, the system includes a substrate that is removable from the container and includes the priming surface. In another embodiment, the container includes a tray having a compartment that receives the applicator. The tray includes a well that includes the priming surface.

Disclosed is a system for reducing or eliminating interference during communication. Disclosed is a system to position an implantable medical device at an orientation or position to reduce or eliminate interference. Therefore, a communication may be maintained with the IMD over a selected period of time.

Methods for treating tissue are provided. In one embodiment, an adjunct material, when secured to tissue, can receive at least one physiological element released from the tissue during healing progression of the tissue, and can exhibit first and second stiffnesses in compression that are approximately constant during first and second time periods from contact with the tissue, with the second stiffness decreasing with time as a function of at least one of oxidation, enzyme-catalyzed hydrolysis, and change of pH resulting from interaction with the at least one physiological element. In another embodiment, the adjunct can receive a unit volume of fluid that causes first and second portions of the adjunct to expand according to first and second expansion behaviors that differ from one another to apply different pressures to the tissue.

A medical device packaging comprises a container having an opening. A medical device is disposed within the container. The medical device includes an adhesive contact face facing the opening. A first cover is disposed over the opening in the container to close the container. A second cover is disposed over the adhesive contact face of the medical device. The first and second covers are connected such that removal of the first cover from the container causes detachment of the second cover from the medical device.

A buttress is applied to an end effector of a surgical stapler. The buttress is loaded on a platform of a buttress applier cartridge. The end effector is closed upon the platform. An adhesive layer of the buttress secures the buttress to the end effector. The buttress is thus adhered to the end effector when the end effector is opened. The end effector is then actuated on tissue of a patient, thereby stapling the buttress to the tissue.

System and methods for out-of-band pairing sterile medical device with non-sterile devices without compromising sterility thereof. A system includes a sterile medical device; a non-sterile computing device; at least one near field communication (NFC) tag; and a sterile packaging enclosing the sterile medical device. In one example, a sterile percutaneous needle guidance device needs to pair and communicate with a non-sterile computer. The sterile device has an NFC tag embedded in the sterile device and an NFC tag embedded in the sterile packaging. The two NFC tags include identification information duplicate of each other. Before opening the sterile packaging either NFC tag can be scanned with the non-sterile device to initiate wireless pairing. If the sterile package is opened before pairing, the NFC tag contained in the packaging can be brought out of the sterile field and scanned with the non-sterile computer thus preserving the sterility of the sterile device.